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Xiongbin Lu, PhD

Present Title & Affiliation

Primary Appointment

Associate Professor, Department of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, TX

Dual/Joint/Adjunct Appointment

Member of the Graduate Faculty, The University of Texas Graduate School of Biomedical Sciences, Houston, TX

Research Interests

Genomic DNA of human cells is under the constant attack of chemicals, free radicals, and UV or ionizing radiation from environmental exposure, by-products of intracellular metabolism, or medical therapy. In response to diverse genotoxic stresses, cells activate DNA damage checkpoint pathways to protect genomic integrity and promote survival of the organism. DNA damage response are a cascade of phosphorylation events initiated by the activation of phosphoinositide 3-kinase (PI3K)-related protein kinases including ATM, ATR and DNA-PK. A vast network of over 700 ATM/ATR targets have been identified and shown to play pivotal roles in the complex cellular response to DNA damage.

In my labortory, we are interested to identify and investigate regulators that modulate the activity of the DNA damage response. Current areas of emphasis include:

(1) Biological functions of the oncogenic Wip1 phosphatase in tumor progression;

(2) Regulation of protein phosphatases and deubiquitinases in the p53-Mdm2 auto-regulatory feedback loop;

(3) Regulation of miRNA and other non-coding RNAs in the DNA damage response.

A combined approach of proteomics, genomics and mouse cancer models will be used in our studies.

Office Address

The University of Texas MD Anderson Cancer Center
7777 Knight Road
Unit Number: 173
Houston, TX 77054
Room Number: Smith Research Building, SRB1.705
Phone: 713-745-6247

Education & Training

Degree-Granting Education

1998 Shanghai Institute of Biochemistry, Chinese Academy of Sciences, Shanghai, China, PHD, Biochemistry
1993 Zhejiang University, Hangzhou, Zhejiang, China, BS, Biological Sciences


Academic Appointments

Assistant Professor, Department of Cancer Biology, Division of Basic Science Research, The University of Texas MD Anderson Cancer Center, Houston, TX, 12/2010-8/2012
Assistant Professor, University of South Carolina, Columbia, SC, 8/2007-11/2010
Research Assistant Professor, Baylor College of Medicine, Houston, TX, 2003-2007

Professional Memberships

American Association for Cancer Research
member, 2007-present
American Association for the Advancement of Science
member, 2006-present
Society of Chinese Bioscientists in America
Life member, 2010-present

Selected Publications

Peer-Reviewed Original Research Articles

1. Wan G, Zhang X, Langley RR, Liu Y, Hu X, Han C, Peng G, Ellis LM, Jones SN, Lu X. DNA-Damage-Induced Nuclear Export of Precursor MicroRNAs Is Regulated by the ATM-AKT Pathway. Cell Rep 3(6):2100-12, 6/27/2013. e-Pub 6/20/2013. PMID: 23791529.
2. Zhang X, Lu X. Posttranscriptional regulation of miRNAs in the DNA damage response. RNA Biol 8(6):960-3, Nov-Dec, 11/2011. e-Pub 11/1/2011. PMCID: PMC3256419.
3. Wan G, Mathur R, Hu X, Zhang X, Lu X. miRNA response to DNA damage. Trends Biochem Sci 36(9):478-84, 9/2011. e-Pub 7/2011. PMID: 21741842.
4. Zhang X, Berger FG, Yang J, Lu X. USP4 Inhibits p53 through Deubiquitinating and Stabilizing ARF-BP1. EMBO J 30(11):2177-89, 6/1/2011. e-Pub 4/26/2011. PMID: 21522127.
5. Zhang X, Wan G, Berger FG, He X, Lu X. The ATM kinase induces microRNA biogenesis in the DNA damage response. Mol Cell 41(4):371-383, 2/18/2011. PMID: 21329876.
6. Zhang W, Gilstrap K, Wu L, K C RB, Moss MA, Wang Q, Lu X, He X. Synthesis and characterization of thermally responsive Pluronic F127-chitosan nanocapsules for controlled release and intracellular delivery of small molecules. ACS Nano 4(11):6747-59, 11/23/2010. e-Pub 11/1/2010. PMID: 21038924.
7. Zhang X, Wan G, Mlotshwa S, Vance V, Berger FG, Chen H, Lu X. Oncogenic Wip1 phosphatase is inhibited by miR-16 in the DNA damage signaling pathway. Cancer Res 70(18):7176-86, 9/15/2010. e-Pub 7/28/2010. PMCID: PMC2940956.
8. Zhang X, Lin L, Guo H, Yang J, Jones SN, Jochemsen A, Lu X. Phosphorylation and degradation of MdmX is inhibited by Wip1 phosphatase in the DNA damage response. Cancer Res 69(20):7960-8, 10/15/2009. e-Pub 10/6/2009. PMCID: PMC2763051.
9. Lu X, Ma O, Nguyen TA, Jones SN, Oren M, Donehower LA. The Wip1 Phosphatase acts as a gatekeeper in the p53-Mdm2 autoregulatory loop. Cancer Cell 12(4):342-54, 10/2007. PMID: 17936559.
10. Lu X, Nannenga B, Donehower LA. PPM1D dephosphorylates Chk1 and p53 and abrogates cell cycle checkpoints. Genes Dev 19(10):1162-74, 5/15/2005. e-Pub 5/3/2005. PMCID: PMC1132003.
11. Lu X, Bocangel D, Nannenga B, Yamaguchi H, Appella E, Donehower LA. The p53-induced oncogenic phosphatase PPM1D interacts with uracil DNA glycosylase and suppresses base excision repair. Mol Cell 15(4):621-34, 8/27/2004. PMID: 15327777.
12. Tyner SD, Venkatachalam S, Choi J, Jones S, Ghebranious N, Igelmann H, Lu X, Soron G, Cooper B, Brayton C, Hee Park S, Thompson T, Karsenty G, Bradley A, Donehower LA. p53 mutant mice that display early ageing-associated phenotypes. Nature 415(6867):45-53, 1/3/2002. PMID: 11780111.
13. Lu X, Silver J. Ecotropic murine leukemia virus receptor is physically associated with caveolin and membrane rafts. Virology 276(2):251-258, 10/2000. PMID: 11040117.

Last updated: 4/21/2014